Oxygen
Oxygen USP Bulk Liquid
Approved
Approval ID
eec2b17b-4ee5-614d-d055-2ed4aaff3357
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 5, 2023
Manufacturers
FDA
Messer Canada Inc.
DUNS: 201613189
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Oxygen
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52003-011
Application NumberNDA205817
Product Classification
M
Marketing Category
C73594
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 5, 2023
FDA Product Classification
INGREDIENTS (1)
OxygenActive
Quantity: 995 mL in 1 L
Code: S88TT14065
Classification: ACTIB